3-HYDROXY-2-PHENYL-2,3-DIHYDRO-4(1H)-QUINOLINONE

3-HYDROXY-2-PHENYL-2,3-DIHYDRO-4(1H)-QUINOLINONE - Names and Identifiers

Name	3-HYDROXY-2-PHENYL-2,3-DIHYDRO-4(1H)-QUINOLINONE
Synonyms	3-hydroxy-2-phenyl-4(1H)-quinolinone 3-Hydroxy-2-phenyl-1H-quinolin-4-one 3-Hydroxy-2-phenylquinolin-4(1H)-one 4(1H)-Quinolinone, 3-hydroxy-2-phenyl- 3-HYDROXY-2-PHENYL-2,3-DIHYDRO-4(1H)-QUINOLINONE
CAS	31588-18-8

3-HYDROXY-2-PHENYL-2,3-DIHYDRO-4(1H)-QUINOLINONE - Physico-chemical Properties

Molecular Formula	C15H11NO2
Molar Mass	237.26
Melting Point	268-270°C
Storage Condition	2-8°C

3-HYDROXY-2-PHENYL-2,3-DIHYDRO-4(1H)-QUINOLINONE - Risk and Safety

Hazard Class

IRRITANT

3-HYDROXY-2-PHENYL-2,3-DIHYDRO-4(1H)-QUINOLINONE - Upstream Downstream Industry

Downstream Products

N-BENZOYLANTHRANILICACID

3-HYDROXY-2-PHENYL-2,3-DIHYDRO-4(1H)-QUINOLINONE - Introduction

3-HYDROXY-2-PHENYL-2,3-DIHYDRO-4(1H)-QUINOLINONE is an organic compound with the chemical formula C14H11NO2 and a molecular weight of 225.24g/mol. The following is a description of its nature, use, preparation and safety information:

Nature:
-Appearance: 3-HYDROXY-2-PHENYL-2, 3-dihydroxy-4 (1H)-QUINOLINONE is a light yellow to yellow-brown crystalline solid.
-Solubility: It is soluble in alcohol and ether, but has low solubility in water.
-Melting point: About 200-202 ° C.

Use:
- 3-HYDROXY-2-PHENYL-2, 3-dihydroxy-4 (1H)-QUINOLINONE has potential biological activity in the pharmaceutical field.
-It is widely used in drug research and development, can be used as the skeleton or basic structure of drug molecules, and further modified to prepare compounds with specific pharmacological effects.

Method:
- 3-HYDROXY-2-PHENYL-2, 3-dihydroxy-4 (1H)-QUINOLINONE can be synthesized by a synthetic reaction.
-A synthesis method is prepared by the cyanation reaction of quinolinone and the condensation reaction of halogenated alkyl compounds.

Safety Information:
- 3-HYDROXY-2-PHENYL-2,3-DIHYDRO-4(1H)-QUINOLINONE use in organic synthesis Laboratories requires appropriate laboratory safety practices, such as wearing laboratory gloves, goggles, and laboratory coats.
-When in contact, avoid touching the skin directly to prevent allergic reactions.
-During operation, pay attention to the volatility and toxicity of chemicals to ensure that the operation is carried out in a well-ventilated place.
-If the compound is inhaled or ingested, seek medical attention immediately.

Last Update：2024-04-09 02:00:50